首页> 美国卫生研究院文献>Rheumatology (Oxford England) >Long-term follow-up of patients who received repeat-dose rituximab as maintenance therapy for ANCA-associated vasculitis
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Long-term follow-up of patients who received repeat-dose rituximab as maintenance therapy for ANCA-associated vasculitis

机译:接受重复剂量利妥昔单抗作为ANCA相关血管炎维持治疗的患者的长期随访

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摘要

>Objective. ANCA-associated vasculitis (AAV) is characterized by a chronic relapsing course. Rituximab (RTX) is an effective maintenance treatment; however, the long-term outcomes after its discontinuation are unclear. The aim of this study was to explore the long-term outcomes of AAV patients treated with repeat-dose RTX maintenance therapy.>Methods. AAV patients receiving a RTX treatment protocol consisting of an induction and maintenance phase were included. For initial remission induction, RTX was dosed at 1 g every 2 weeks or 375 mg/m2 weekly for 4 consecutive weeks and for remission maintenance at 1 g every 6 months for 24 months. At the first RTX administration, ongoing immunosuppressives were withdrawn.>Results. Sixty-nine patients were identified, 67 of whom were failing other therapies. Nine relapsed during the RTX treatment protocol; however, all 69 were in remission at the end of the maintenance phase on a median prednisolone dose of 2.5 mg/day and 9% were receiving additional immunosuppression. During subsequent observation, 28 patients relapsed a median of 34.4 months after the last RTX infusion. Risk factors for relapse were PR3-associated disease (P = 0.039), B cell return within 12 months of the last RTX infusion (P = 0.0038) and switch from ANCA negativity to positivity (P = 0.0046). Two patients died and two developed severe hypogammaglobulinaemia.>Conclusion. This study supports the efficacy and safety of a fixed-interval RTX maintenance regimen in relapsing/refractory AAV. Relapses after discontinuation of maintenance therapy did occur, but at a lower rate than after a single RTX induction course. PR3-associated disease, the switch from ANCA negative to positive and the return of B cells within 12 months of the last RTX administration were risk factors for further relapse.
机译:>客观。ANCA相关血管炎(AAV)的特征是慢性复发过程。利妥昔单抗(RTX)是一种有效的维持治疗方法;但是,终止后的长期结果尚不清楚。这项研究的目的是探讨重复剂量RTX维持疗法治疗的AAV患者的长期结果。>方法。包括接受RTX治疗方案(包括诱导和维持阶段)的AAV患者。对于最初的缓解诱导,连续2周每2周以1 g剂量或每周375 mg / m 2 给予RTX,并每6个月以1 g维持缓解剂量,持续24个月。首次使用RTX时,撤消了正在进行的免疫抑制剂。>结果。确定了69例患者,其中67例因其他疗法无效。 RTX治疗方案中有9例复发;然而,在维持阶段结束时,所有69例患者都接受了泼尼松龙中位剂量2.5 mg /天的缓解,其中9%的患者接受了额外的免疫抑制。在随后的观察中,有28例患者在最后一次RTX输注后中位复发34.4个月。复发的危险因素是与PR3相关的疾病(P = 0.039),在最后一次RTX输注后12个月内B细胞返回(P = 0.0038)以及从ANCA阴性转为阳性(P = 0.0046)。有2例患者死亡,有2例严重的低丙种球蛋白血症。>结论。该研究支持固定间隔RTX维持方案在复发性/难治性AAV中的有效性和安全性。停止维持治疗后确实发生了复发,但复发率低于单个RTX诱导疗程后。与PR3相关的疾病,从ANCA阴性转为阳性以及在最近一次RTX给药后12个月内B细胞返回是进一步复发的危险因素。

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